rs74085882
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs74085882(C;C) |
Make rs74085882(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 51944251 |
Gene | ATP7B |
is a | snp |
is | mentioned by |
dbSNP | rs74085882 |
dbSNP (classic) | rs74085882 |
ClinGen | rs74085882 |
ebi | rs74085882 |
HLI | rs74085882 |
Exac | rs74085882 |
Gnomad | rs74085882 |
Varsome | rs74085882 |
LitVar | rs74085882 |
Map | rs74085882 |
PheGenI | rs74085882 |
Biobank | rs74085882 |
1000 genomes | rs74085882 |
hgdp | rs74085882 |
ensembl | rs74085882 |
geneview | rs74085882 |
scholar | rs74085882 |
rs74085882 | |
pharmgkb | rs74085882 |
gwascentral | rs74085882 |
openSNP | rs74085882 |
23andMe | rs74085882 |
SNPshot | rs74085882 |
SNPdbe | rs74085882 |
MSV3d | rs74085882 |
GWAS Ctlg | rs74085882 |
GMAF | 0.001377 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs74085882(C;C) |
Alt | rs74085882(C;C) |
Reference | Rs74085882(T;T) |
Significance | Other |
Disease | Wilson disease not specified |
Variation | info |
Gene | ATP7B |
CLNDBN | Wilson disease not specified |
Reversed | 0 |
HGVS | NC_000013.10:g.52518387T>C |
CLNSRC | ClinVar LabCorp University of Washington |
CLNACC | RCV000029368.3, RCV000244000.2, |